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3-Quinuclidinyl benzilate (agent BZ) toxicokinetics in rats

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F21%3A10430279" target="_blank" >RIV/00216208:11150/21:10430279 - isvavai.cz</a>

  • Alternative codes found

    RIV/60162694:G44__/21:00557158 RIV/00216208:11160/21:10430279

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=YNmOcUa0ec" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=YNmOcUa0ec</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/bcpt.13627" target="_blank" >10.1111/bcpt.13627</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    3-Quinuclidinyl benzilate (agent BZ) toxicokinetics in rats

  • Original language description

    3-Quinuclidinyl benzilate (BZ) ranks among incapacitating military warfare agents. It acts as a competitive inhibitor on muscarinic receptors leading to non-lethal mental impairment. The present study aimed to investigate toxicokinetics of BZ in rats. Moreover, BZ can be exploited to produce a pharmacological model of Alzheimer&apos;s disease; thus, this paper focuses mainly on the BZ distribution to the brain. Wistar rats were administered i.p. with BZ (2 and 10 mg/kg). The BZ concentration was determined using LC-MS/MS in plasma, urine, bile, brain, kidney and liver. The sample preparation was based on a solid phase extraction (liquids) or protein precipitation (organ homogenates). The plasma concentration peaked at 3 min (204.5 +/- 55.4 and 2185.5 +/- 465.4 ng/ml). The maximal concentration in the brain was reached several minutes later. Plasma elimination half-life was 67.9 +/- 3.4 in the 2 mg/kg group and 96.6 +/- 27.9 in the 10 mg/kg group. BZ concentrations remained steady in the brain, with slow elimination (t(1/2) 506.9 +/- 359.5 min). Agent BZ is excreted mainly via the urine. Steady BZ concentration in the brain could explain the previously published duration of the significant impairment in passive avoidance tasks in rats after an injection of BZ.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Basic &amp; Clinical Pharmacology &amp; Toxicology

  • ISSN

    1742-7835

  • e-ISSN

  • Volume of the periodical

    129

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    246-255

  • UT code for WoS article

    000668041800001

  • EID of the result in the Scopus database

    2-s2.0-85108981136